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Plasma polymer films are more and more used in numerous applications such as the day-to-day packaging, which requires a good mechanical resistance of the coating. Since mechanical properties are function of the cross-linking degree of the thin films, it is important to understand the relationship between the two. In this work, plasma polymer films were studied in terms of cross-linking degree and mechanical properties, measured by means of ToF-SIMS coupled to PCA and depth-sensing nanoindentation, respectively. The data reveal that when the power increases, the films are more cross-linked and show higher hardness, higher elastic recovery, lower creep strain and an increased ability for self-healing. As the plasma polymer films are more cross-linked, the plasticity drops and the viscoelasticity and hardness increase. [ABSTRACT FROM AUTHOR]

In this work, a new plasma diagnostic method has been used to quantify the plasma-generated species that play a part in the ethyl lactate plasma polymer film deposition. This method has been possible by using the RGA mass spectrometry combined with the in situ FTIR spectroscopy supported by DFT calculations. Ethyl lactate plasma phase can then be qualitatively and quantitatively probed by varying the experimental parameters. More specifically, it has been shown that by increasing the power from 30 to 280 W, the density of ester-bearing species in the plasma strongly decreases and supports the drop of ester content in plasma polymers. Additionally, the temperature of the plasma has been determined by the in situ IR spectroscopy and has revealed a too weak increase (60 K) to affect the fundamental vibrational levels. Our IR spectroscopy approach goes into that direction too. [ABSTRACT FROM AUTHOR]

In this work, we report on the synthesis of ethyl lactate-based plasma polymer film (ELPPF) by plasma enhanced chemical vapour deposition (PECVD). Using a design of experiments, it appears that, among other, the injected power ( PRF) is the key parameter affecting the ELPPF features. Indeed, we observe a strong decrease of the COO-C/H functionalities (from 12 to 2 at.%) within a limited PRF domain. A more precise analysis of the film chemistry by combining XPS and chemical derivatization reveals that up to 95% of these carboxyl-based functions are esters. On the other hand, we show that the cross-linking degree of the ELPPF can be increased by a factor of two as a function of PRF. This work paves the way for the tailoring of the barrier properties of ELPPF by controlling the ester content and the cross-linking degree of the PPF. [ABSTRACT FROM AUTHOR]